Mutation - lon-11

Mutation - lon-11Mutation lon-11

Mutation lon-11

Name: lon-11
Type: Other
Mutation of Gene: lon
Approx. Map Location: 9.88
Synonyms
Designation Where Used
lon-11
Comments
- is a mutation of an E. coli B gene caused by an IS186 insertion in the promoter. All derivatives of Witkin's B wildtype carry this lon mutation.
References

15 Strains Carrying This Mutation

Name	Mutations	Genotype
BA-002	3	F-, lon-11, Δ(ompT-nfrA)885, Δ(galM-ybhJ)884, λDE3 [lacI, lacUV5-T7 gene 1, ind1, sam7, nin5], Δ46, ?ptsI845::FRT, [mal⁺]_K-12(λ^S), hsdS10
WP2	3	F-, lon-11, sulA1, trpE65(Oc)
CM1320	4	F-, lon-11, sulA1, trpE65(Oc), mutM102::kan
E. coli B/r	4	F-, lon-11, sulA1, λ^R, Mal(ts)
F26	4	F-, lon-11, sulA1, his-222, thyA751
WP2 hcr^-	4	F-, lon-11, sulA1, trpE65(Oc), uvrA155
WU38	4	F-, lon-11, sulA1, tyrA14, recA1
BS21	5	F-, lon-11, sulA1, his-222, thyA751, adc-1
BL21(DE3)	7	F-, lon-11, Δ(ompT-nfrA)885, Δ(galM-ybhJ)884, λDE3 [lacI, lacUV5-T7 gene 1, ind1, sam7, nin5], Δ46, [mal⁺]_K-12(λ^S), hsdS10
BL21(DE3)/pCP20	7	F-, lon-11, Δ(ompT-nfrA)885, Δ(galM-ybhJ)884, λDE3 [lacI, lacUV5-T7 gene 1, ind1, sam7, nin5], Δ46, [mal⁺]_K-12(λ^S), hsdS10, pCP20
BL21(DE3)/pKD46	7	F-, lon-11, Δ(ompT-nfrA)885, Δ(galM-ybhJ)884, λDE3 [lacI, lacUV5-T7 gene 1, ind1, sam7, nin5], Δ46, [mal⁺]_K-12(λ^S), hsdS10, pKD46
BL21(DE3)/pLysS	7	F-, lon-11, Δ(ompT-nfrA)885, Δ(galM-ybhJ)884, λDE3 [lacI, lacUV5-T7 gene 1, ind1, sam7, nin5], Δ46, [mal⁺]_K-12(λ^S), hsdS10, pLysS
HB4	8	F-, thr-11, leuB19, lac-12, lon-11, sulA1, rpsL56(strR), gal-13, pro-19
HB45	13	F-, thr-11, leuB19, lac-11, lon-11, sulA1, trp-25, rpsL56(strR), rbs-20, his-47, met-55, arg-28, pro-19, gal-11
WM437	14	F-, leuB19, lac-11, lon-11, sulA1, trp-25, dnaI208(ts), thyA59, rpsL56(strR), deoB23, gal-11, pro-19, met-55, arg-28, his-47